scholarly journals Isolating Polaritonic 2D-IR Transmission Spectra

Author(s):  
Rong Duan ◽  
Joseph N. Mastron ◽  
Yin Song ◽  
Kevin J. Kubarych
MRS Advances ◽  
2020 ◽  
Vol 5 (52-53) ◽  
pp. 2661-2667 ◽  
Author(s):  
Puja Goel ◽  
Manju Arora

AbstractSuccessful disintegration of Chlorpyrifos pesticide by nearly monodisperse nano-gold photcatalyst (∼10 nm) for remediation of wastewater has been reported in current studies. Nano-Gold dispersion reaction with Chlorpyrifos solutions completes in 45 minutes at ambient temperature under the normal daylight and exhibit systematic variations in the solution color from wine red to pink to light sky blue and finally transforming into a transparent solution with fine precipitates. UV-Vis absorption studies correlates well with the systematic color changes as observed in the nano-gold treated Chlorpyrifos solutions with time. The characteristic localized surface plasmon resonance peak of nanogold dispersion observed at 529 nm red shifts to weak, medium and strong intensity peaks at ∼ 640 nm, 740 nm and 890 nm on increasing chlorpyrifos concentration owing to the aggregation of gold nanoparticles in small to bigger sized clusters. The fine turbidity in final transparent solution further confirms the aggregation of nanogold particles into stable bigger ensembles. IR transmission spectra of final transparent solutions showed disappearance of Chlorpyrifos νC-Cl and phosphorothioate functional group peaks indicating degradation of chlorpyrifos.


2003 ◽  
Vol 20 (9) ◽  
pp. 1600-1602 ◽  
Author(s):  
Li Guo-Qiang ◽  
Jie Wan-Qi ◽  
Gu Zhi ◽  
Hua Hui

2011 ◽  
Vol 103 ◽  
pp. 458-463
Author(s):  
Xun Si Wang ◽  
Jie Sun ◽  
Qiu Hua Nie ◽  
Shi Xun Dai ◽  
Xiang Hua Zhang ◽  
...  

In order to decrease the impurity absorption bands of Ge-Se-Te chalcogenide glasses in IR region. Three different kinds of deoxidants including Mg(magnesium), Al(aluminium) and Ca(calcium) were chosen. Properties measurements including density, Vis-NIR and infrared (IR) transmission spectra were adopted to analyze the relationship between impurity absorption bands and deoxidants. The concentrations of impurities in glass samples with different content of Mg were calculated by method of optic spectra. The results show that Mg is a better choice as deoxidant for chalcogenide glasses compared to Al and Ca. The values of main impurity concentration decrease from 4417.833 to 0 ppmw for Ge-O and from 55.236 to 0 ppmw for Si-O with increasing content of Mg, respectively. At least 200ppm Mg is needed to minimize the main absorption bands in IR region and G5 glass incorporated with 400ppm Mg has minimum concentration of impurities which means that it possesses the optimal transmission properties.


1997 ◽  
Vol 51 (8) ◽  
pp. 1170-1175 ◽  
Author(s):  
Shinri Sato ◽  
Toshihiro Suzuki

IR transmission spectra were measured in an ultrahigh vacuum system for Fe(CO)5, n-decane, and NH3 adsorbed at <150 K on transparent Au films evaporated on a sapphire plate. The spectra of Fe(CO)5 show ∼10-fold enhancement as compared to those observed on an SiO2 lm coated on a sapphire plate, which has been reported as surface-enhanced IR-absorption (SEIRA). The enhancement is reduced when the coverage of adsorbate exceeds a mono-layer or other molecules present on the surface prior to adsorption, indicating that SEIRA is effective only in the close vicinity of the surface. The SEIRA effect is also reduced when film is heated in a vacuum, probably because of sintering of the Au particles forming the film. In addition, the heat treatment of the film results in blue shifts of bands, accompanied by some band distortion. With the use of SEIRAS, the surface photochemistry of Fe(CO)5 has been investigated.


1986 ◽  
Vol 40 (4) ◽  
pp. 427-434 ◽  
Author(s):  
John E. Bertie ◽  
R. Norman Jones ◽  
Victor Behnam

This paper completes the report of our FT-IR measurements of transmission spectra of organic liquids. These measurements were undertaken in order to estimate the photometric accuracy of our FT-IR spectrometer for transmission spectra by comparing the results with those measured previously [Applied Spectroscopy 34, 657 (1980)] by a calibrated dispersive spectrometer. We have studied 97 bands of chlorobenzene, toluene, and dichloromethane, in 500-μm cells and 54 bands of benzene, chlorobenzene, toluene, cyclopentane, and dichloromethane, in cells 11 to 53 μm thick. The average value of the imaginary refractive index at the band peak, kmax, is reported for each band and compared with the calibrated value. When averaged over the 184 bands that are reported in this work and our earlier paper [Applied Spectroscopy 39, 401 (1985)], our measurements agree with the calibrated values to about 3% of kmax, and have a 90% confidence limit of about 0.7 to 1% of kmax, The calibrated values themselves have an estimated error of about 6%, so to obtain better knowledge of the accuracy of our measurements we need better standards and we need measurements to be made on other FT-IR instruments. We plan to publish simplified procedures that will encourage others to make such measurements. Our 90% confidence limit includes effects due to the use of different cells, daily realignment of the fixed mirror of the interferometer, realignment of the optics of the detector and sample compartments, change of beamsplitter, and a day-to-day variation of uncertain origin, in addition to the error sources that always contribute to typical analytical precision. Our data do not show these additional error sources to be systematic, so it is appropriate to include their effect in the evaluation of the confidence limit. We believe the main source of error to be the effect of the infrared cell on the path of the light beam through the instrument. The day-to-day variation of uncertain origin is thought to be due to very small changes in the beam path through the instrument, which in turn cause the effect of the infrared cell on the beam to vary.


2018 ◽  
Vol 32 (27) ◽  
pp. 1850328
Author(s):  
Li Dai ◽  
Xianbo Han ◽  
Yu Shao ◽  
Luping Wang ◽  
Chunrui Liu ◽  
...  

The Sc:Fe:Cu:LiNbO3 crystals were grown with Fe[Formula: see text](0.3 wt.%), Cu[Formula: see text](0.1 wt.%) and Sc[Formula: see text](1 mol.%) by the Czochralski method with various [Li]/[Nb] ratios (0.946, 1.05, 1.20 and 1.38). The influence of the [Li]/[Nb] ratios on the defect structure of Sc:Fe:Cu:LiNbO3 crystals was analyzed by the UV-Visible spectra and IR transmission spectra. The spectra show that the absorption edge shift to the red with [Li]/[Nb] ratios enhancing. The Sc:Fe:Cu:LiNbO3 crystals with [Li]/[Nb] ratio of 1.05 is nearly stoichiometric. A new narrow OH[Formula: see text] associated vibrational peak at 3505 cm[Formula: see text] was revealed in Sc:Fe:Cu:LiNbO3 crystals with the ratio of [Li]/[Nb] = 1.38. It is attributed to the (Sc[Formula: see text])-(OH)[Formula: see text]. The results show that the defect structure changes with the [Li]/[Nb] ratios variation.


2008 ◽  
Vol 600-603 ◽  
pp. 441-444 ◽  
Author(s):  
Frank Schmid ◽  
Kurt Semmelroth ◽  
Michael Krieger ◽  
Heiko B. Weber ◽  
Gerhard Pensl ◽  
...  

6H-SiC was doped with phosphorus (P) donors by neutron transmutation. IR transmission spectra were taken in the temperature range from 6 K to 300 K. A great number of absorption lines is observed at temperatures below 140 K; these lines are attributed to transitions of the donor electron between ground states and bound excited states of P-related donors. Based on Faulkner's theory, three series of effective-mass-like states (P1, P2, P3) could be identified. The corresponding ground state energies are: E(P1) = EC - 91.5 meV, E(P2) = EC - 81.8 meV, E(P3) = EC - 73.5 meV.


Sign in / Sign up

Export Citation Format

Share Document